Ongoing Monitoring of Vital Signs in Patients With Idiopathic Pulmonary Fibrosis Before and After Acute Exacerbation. (REACT)

Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY

The aim of this study is to assess the feasibility of early detection of acute exacerbations of idiopathic pulmonary fibrosis by the remote monitoring of vital signs. The main question the study aims to answer is: Could a remote monitoring device allow for earlier detection of exacerbations with individualized monitoring and continuous data collection? All patients will receive conventional clinical follow-up based on their health status and clinical recommendations. At the same time, they will benefit from the Bora Care® medical remote monitoring device.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patient over 18 years of age, ideally 50% male and 50% female

• Patient with IPF with a known level of respiratory function (EFR and blood gas less than 3 months)

• Stable patient, i.e. without hospitalisation or exacerbation in the last 3 months

• Patient desaturating at 6MW in ambient air (AA) and requiring ambulatory oxygen therapy (SpO2 AA ⩽ 88%)

• Patient not receiving walking or permanent oxygen therapy at baseline

• Informed patient who has signed consent

• Patient affiliated to a social security scheme

• Patient not monitored by a home healthcare provider other than Air de Bretagne.

Locations
Other Locations
France
Chru Pontchaillou
RECRUITING
Rennes
Contact Information
Primary
Alexis TOULLEC
clinical@biosency.com
02 21 65 70 01
Time Frame
Start Date: 2024-06-17
Estimated Completion Date: 2026-02
Participants
Target number of participants: 30
Sponsors
Collaborators: Association Fibroses Pulmonaires France, Rennes University Hospital, Air de Bretagne
Leads: Biosency

This content was sourced from clinicaltrials.gov